A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190911



Internal ID22341700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9937297..9937402hg38UCSC Ensembl
chr12:10089896..10090001hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14441777
SamplesHG00733
Known GenesLOC102467076
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190911
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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